Schuster Julian A, Vogel Rudi F, Ehrmann Matthias A
Lehrstuhl für Technische Mikrobiologie, Technische Universität München, Gregor-Mendel-Str. 4, 85354, Freising, Germany.
Arch Microbiol. 2019 Apr;201(3):337-347. doi: 10.1007/s00203-019-01619-x. Epub 2019 Jan 11.
Clustered regularly interspaced palindromic repeats (CRISPR)-Cas (CRISPR-associated) structures, known as prokaryotes 'immune system', have been successfully applied for genetic engineering and genotyping purposes for a variety of microorganisms. Here we investigated 50 Lactobacillus (L.) sakei genomes and found 13 of them as CRISPR-Cas positive. The majority of positive genomes contain type II-A system, which appears to be widespread across food born lactic acid bacteria. However, a type II-C system with low similarity in Cas protein sequence to related II-C structures is rarely present in the genomes. We depicted a correlation between prophages integrated in the genomes and the presence/absence of CRISPR-Cas systems and identified the novel protospacer adjunction motifs (PAMs) (a/g)AAA for the II-A and (g/a)(c/t)AC for the II-C system including the corresponding tracrRNAs, creating the basis for the development of new Cas-mediated genome editing tools. Moreover, we performed a PCR screening for 81 selected L. sakei isolates and identified 25 (31%) isolates as CRISPR-Cas positive with hypervariable spacer content. Comparative sequence analysis of 33 repeat-spacer arrays resulted in 18 CRISPR genotypes, revealing insights into evolutionary relationships between different strains and illustrating possible applications for the research and development of starter cultures, e.g., the usage for strain differentiation in assertiveness experiments or the development of bacteriophage-resistant strains.
成簇规律间隔短回文重复序列(CRISPR)-Cas(CRISPR相关)结构,即原核生物的“免疫系统”,已成功应用于多种微生物的基因工程和基因分型。在此,我们研究了50个清酒乳杆菌基因组,发现其中13个为CRISPR-Cas阳性。大多数阳性基因组含有II-A型系统,该系统似乎在食源性乳酸菌中广泛存在。然而,Cas蛋白序列与相关II-C结构相似度较低的II-C型系统在基因组中很少见。我们描述了整合在基因组中的原噬菌体与CRISPR-Cas系统的存在与否之间的相关性,并确定了II-A型系统的新型原间隔相邻基序(PAM)(a/g)AAA和II-C型系统的(g/a)(c/t)AC,包括相应的反式激活crRNA,为开发新的Cas介导的基因组编辑工具奠定了基础。此外,我们对81株选定的清酒乳杆菌分离株进行了PCR筛选,鉴定出25株(31%)分离株为CRISPR-Cas阳性,其间隔序列具有高变异性。对33个重复间隔序列阵列的比较序列分析产生了18种CRISPR基因型,揭示了不同菌株之间的进化关系,并说明了其在发酵剂研发中的可能应用,例如在特性实验中用于菌株鉴别或开发抗噬菌体菌株。